Neonatal Graves Disease Masquerading as Hemochromatosis

dc.contributor.authorMaggiotto, Liesbeth
dc.contributor.authorMittelman, Steven D.
dc.contributor.authorFallah, Roja
dc.contributor.departmentPediatrics, School of Medicine
dc.date.accessioned2024-09-16T10:18:44Z
dc.date.available2024-09-16T10:18:44Z
dc.date.issued2024-07-24
dc.description.abstractThyroid autoimmunity is extremely common in the adult population and can affect pregnancy outcomes. Signs in the newborn can range from absent to severe, making the diagnosis easy to miss. We present an interesting case of neonatal Graves disease associated with intrauterine growth restriction, premature delivery, and liver failure with severely high ferritin, thought to be secondary to hemochromatosis. Treatment of the underlying hyperthyroidism caused a rapid resolution of the elevated ferritin and liver failure. This report highlights the importance of considering Graves disease in newborns with liver failure of unknown etiology.
dc.eprint.versionFinal published version
dc.identifier.citationMaggiotto L, Mittelman SD, Fallah R. Neonatal Graves Disease Masquerading as Hemochromatosis. JCEM Case Rep. 2024;2(7):luae132. Published 2024 Jul 24. doi:10.1210/jcemcr/luae132
dc.identifier.urihttps://hdl.handle.net/1805/43319
dc.language.isoen_US
dc.publisherOxford University Press
dc.relation.isversionof10.1210/jcemcr/luae132
dc.relation.journalJCEM Case Reports
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectNeonatal Graves disease
dc.subjectFerritin
dc.subjectLiver enzymes
dc.subjectThyroid disease
dc.subjectHemochromatosis
dc.titleNeonatal Graves Disease Masquerading as Hemochromatosis
dc.typeArticle
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